6979-94-8 | 2',3',5'-Triacetylguanosine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$12.00	$9.00
5g	95%	in stock	$29.00	$21.00
25g	95%	in stock	$75.00	$53.00
500g	95%	in stock	$1,179.00	$825.00

Description

• Catalog Number: AB59767
• Chemical Name: 2',3',5'-Triacetylguanosine
• CAS Number: 6979-94-8
• Molecular Formula: C16H19N5O8
• Molecular Weight: 409.3508
• MDL Number: MFCD00057054
• SMILES: CC(=O)O[C@@H]1[C@H](OC(=O)C)[C@H](O[C@H]1n1cnc2c1nc(N)[nH]c2=O)COC(=O)C

Computed Properties

• Complexity: 743
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 4
• Heavy Atom Count: 29
• Hydrogen Bond Acceptor Count: 10
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 8
• XLogP3: -0.7

Literature

• Structure and gelation mechanism of tunable guanosine-based supramolecular hydrogels.

  Langmuir : the ACS journal of surfaces and colloids 20100615

• Oxidative modification of guanine bases initiated by oxyl radicals derived from photolysis of azo compounds.

  The journal of physical chemistry. B 20100520

• Tailoring the properties of guanosine-based supramolecular hydrogels.

  Langmuir : the ACS journal of surfaces and colloids 20090804

• Pathways of arachidonic acid peroxyl radical reactions and product formation with guanine radicals.

  Chemical research in toxicology 20080201

• Oxidative generation of guanine radicals by carbonate radicals and their reactions with nitrogen dioxide to form site specific 5-guanidino-4-nitroimidazole lesions in oligodeoxynucleotides.

  Chemical research in toxicology 20030801

• Peroxynitrite-induced reactions of synthetic oligo 2'-deoxynucleotides and DNA containing guanine: formation and stability of a 5-guanidino-4-nitroimidazole lesion.

  Biochemistry 20020611

• A novel nitroimidazole compound formed during the reaction of peroxynitrite with 2',3',5'-tri-O-acetyl-guanosine.

  Journal of the American Chemical Society 20011212